Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Hydromorphone Hydrochloride | HCID 5462347 | — |
| Product | HCID 117857408 | HCID 117857408 | 99.9% |
Reaction Steps
To Hydromorphone HCl (15.0 g, 46.7 mmol) was added ethylene glycol (80 mL) and methane sulfonic acid (10 mL) and the reaction heated at 80° C. overnight. The reaction was cooled to room temperature and poured into ice/NH3(aq) (˜350 mL). The product was extracted with dichloromethane and dried over MgSO4 before concentration under reduced pressure to give (4R,4aR,7aR,12bS)-3-methyl-1,2,3,4,4a,5,6,7a-octahydrospiro[4,12-methanobenzofuro[3,2-e]isoquinoline-7,2′-[1,3]dioxolan]-9-ol (19 g, 99.9% LCMS); [M+H]+ 330.5. This was taken onto the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09416137B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-55877d2c5b9c439cb8e48370652ed9c8 |
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| Source note | uspto-grants-2016_08 |
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